rs63750097

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Lynch syndrome, pathogenic mutation

Make rs63750097(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414338

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750097
dbSNP (classic)	rs63750097
ClinGen	rs63750097
ebi	rs63750097
HLI	rs63750097
Exac	rs63750097
Gnomad	rs63750097
Varsome	rs63750097
LitVar	rs63750097
Map	rs63750097
PheGenI	rs63750097
Biobank	rs63750097
1000 genomes	rs63750097
hgdp	rs63750097
ensembl	rs63750097
geneview	rs63750097
scholar	rs63750097
google	rs63750097
pharmgkb	rs63750097
gwascentral	rs63750097
openSNP	rs63750097
23andMe	rs63750097
SNPshot	rs63750097
SNPdbe	rs63750097
MSV3d	rs63750097
GWAS Ctlg	rs63750097

Max Magnitude

6

ClinVar
Risk	rs63750097(T;T)
Alt	rs63750097(T;T)
Reference	Rs63750097(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47641477C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076738.2, RCV000484173.1,